3β-acetoxy-3'-methyl-(16β,17β)-16,17-dihydro-androst-5-eno[17,16-d]isoxazole结构式
|
常用名 | 3β-acetoxy-3'-methyl-(16β,17β)-16,17-dihydro-androst-5-eno[17,16-d]isoxazole | 英文名 | 3β-acetoxy-3'-methyl-(16β,17β)-16,17-dihydro-androst-5-eno[17,16-d]isoxazole |
|---|---|---|---|---|
| CAS号 | 1053-36-7 | 分子量 | 371.51300 | |
| 密度 | 1.31g/cm3 | 沸点 | 461ºC at 760 mmHg | |
| 分子式 | C23H33NO3 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 159.5ºC |
| 英文名 | 3β-acetoxy-3'-methyl-(16β,17β)-16,17-dihydro-androst-5-eno[17,16-d]isoxazole |
|---|---|
| 英文别名 | 更多 |
| 密度 | 1.31g/cm3 |
|---|---|
| 沸点 | 461ºC at 760 mmHg |
| 分子式 | C23H33NO3 |
| 分子量 | 371.51300 |
| 闪点 | 159.5ºC |
| 精确质量 | 371.24600 |
| PSA | 47.89000 |
| LogP | 4.31730 |
| InChIKey | XHKXOQIVQHCQQV-UHFFFAOYSA-N |
| SMILES | CC(=O)OC1CCC2(C)C(=CCC3C2CCC2(C)C3CC3ON=C(C)C32)C1 |
| 蒸汽压 | 1.11E-08mmHg at 25°C |
| 折射率 | 1.648 |
|
~%
3β-acetoxy-3'-m... 1053-36-7 |
| 文献:Kaufmann,S. et al. Journal of Organic Chemistry, 1969 , vol. 34, # 6 p. 1618 - 1621 |
|
~%
3β-acetoxy-3'-m... 1053-36-7 |
| 文献:Kaufmann,S. et al. Journal of Organic Chemistry, 1969 , vol. 34, # 6 p. 1618 - 1621 |
| 上游产品 1 | |
|---|---|
| 下游产品 0 | |
|
实验名称:Luminescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id:OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
|
|
实验名称:QFRET-based biochemical primary high throughput screening assay to identify exosite i...
来源:The Scripps Research Institute Molecular Screening Center
靶标:disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id:ADAM17_INH_QFRET_1536_1X%INH PRUN
|
|
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_AG_FLUO8_1536_1X%ACT PRUN
|
|
实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1100
|
|
实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1101
|
|
实验名称:Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Bas...
来源:Broad Institute
靶标:N/A
External Id:2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2
|
|
实验名称:Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
来源:Broad Institute
靶标:FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id:2147-01_Inhibitor_SinglePoint_HTS_Activity
|
|
实验名称:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
来源:Broad Institute
靶标:N/A
External Id:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
|
|
实验名称:High throughput screen for small molecule inhibitors of a hypoxia-regulated fluoresce...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:N/A
External Id:HMS1149-MLP
|
|
实验名称:qHTS for Inhibitors of AMA1-RON; Towards Development of Antimalarial Drug Lead: Prima...
来源:NCGC
靶标:apical membrane antigen 1, AMA1 [Plasmodium falciparum 3D7]
External Id:AMA1100
|
| hms3087c07 |